TWI254068B - Thermosetting coating materials - Google Patents

Thermosetting coating materials Download PDF

Info

Publication number: TWI254068B
Authority: TW; Taiwan
Prior art keywords: acid; coating material; patent application; aliphatic; scope
Prior art date: 2000-01-31

Application number

TW090101825A

Other languages

English (en)

Chinese (zh)

Inventor

Andreas Kaplan

Albert Reich

Original Assignee

Ems Chemie Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-01-31

Filing date

2001-01-30

Publication date

2006-05-01

2001-01-30 Application filed by Ems Chemie Ag filed Critical Ems Chemie Ag

2006-05-01 Application granted granted Critical

2006-05-01 Publication of TWI254068B publication Critical patent/TWI254068B/zh

Links

238000000576 coating method Methods 0.000 title claims abstract description 28
239000011248 coating agent Substances 0.000 title claims abstract description 23
239000000463 material Substances 0.000 title claims abstract description 16
229920001187 thermosetting polymer Polymers 0.000 title claims abstract description 6
229920000728 polyester Polymers 0.000 claims abstract description 11
239000000654 additive Substances 0.000 claims abstract description 4
239000000945 filler Substances 0.000 claims abstract description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 17
239000000843 powder Substances 0.000 claims description 17
239000002253 acid Substances 0.000 claims description 13
238000004519 manufacturing process Methods 0.000 claims description 9
239000000203 mixture Substances 0.000 claims description 9
125000001931 aliphatic group Chemical group 0.000 claims description 6
229920006395 saturated elastomer Polymers 0.000 claims description 6
239000000126 substance Substances 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 5
229920000058 polyacrylate Polymers 0.000 claims description 5
229920000642 polymer Polymers 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
150000001875 compounds Chemical class 0.000 claims description 3
239000004615 ingredient Substances 0.000 claims description 3
239000000049 pigment Substances 0.000 claims description 3
238000006116 polymerization reaction Methods 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
150000008065 acid anhydrides Chemical class 0.000 claims description 2
125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 2
238000009472 formulation Methods 0.000 claims description 2
125000000962 organic group Chemical group 0.000 claims description 2
239000002245 particle Substances 0.000 claims description 2
229920005862 polyol Polymers 0.000 claims description 2
150000003077 polyols Chemical class 0.000 claims description 2
238000007639 printing Methods 0.000 claims description 2
230000000996 additive effect Effects 0.000 claims 1
239000002518 antifoaming agent Substances 0.000 claims 1
238000006482 condensation reaction Methods 0.000 claims 1
150000002431 hydrogen Chemical group 0.000 claims 1
239000011241 protective layer Substances 0.000 claims 1
239000002689 soil Substances 0.000 claims 1
239000003017 thermal stabilizer Substances 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 abstract description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 3
239000004608 Heat Stabiliser Substances 0.000 abstract 1
238000007872 degassing Methods 0.000 abstract 1
-1 alkyl decylamines Chemical class 0.000 description 17
239000000178 monomer Substances 0.000 description 11
229920001577 copolymer Polymers 0.000 description 10
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
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KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
238000000034 method Methods 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
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150000002978 peroxides Chemical class 0.000 description 5
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ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical group CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 3
238000007334 copolymerization reaction Methods 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 3
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 3
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 3
239000007858 starting material Substances 0.000 description 3
ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 description 2
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
229920002125 Sokalan® Polymers 0.000 description 2
244000028419 Styrax benzoin Species 0.000 description 2
235000000126 Styrax benzoin Nutrition 0.000 description 2
235000008411 Sumatra benzointree Nutrition 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
229960002130 benzoin Drugs 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
230000002079 cooperative effect Effects 0.000 description 2
230000000875 corresponding effect Effects 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
125000004185 ester group Chemical group 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
235000019382 gum benzoic Nutrition 0.000 description 2
CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical compound CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000012768 molten material Substances 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
239000004584 polyacrylic acid Substances 0.000 description 2
CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
238000003756 stirring Methods 0.000 description 2
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
239000000052 vinegar Substances 0.000 description 2
235000021419 vinegar Nutrition 0.000 description 2
BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
POBUJEBYLIZDCQ-UHFFFAOYSA-N 1,2,3-tributyl-4-propan-2-ylbenzene Chemical compound C(CCC)C1=C(C(=C(C=C1)C(C)C)CCCC)CCCC POBUJEBYLIZDCQ-UHFFFAOYSA-N 0.000 description 1
DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
JOFQXPUKJJQCPW-UHFFFAOYSA-N 1-methyl-1-propylhydrazine Chemical compound CCCN(C)N JOFQXPUKJJQCPW-UHFFFAOYSA-N 0.000 description 1
229940114072 12-hydroxystearic acid Drugs 0.000 description 1
OOHZIRUJZFRULE-UHFFFAOYSA-N 2,2-dimethylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(C)C OOHZIRUJZFRULE-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
YVVVNAZSGGAAPW-UHFFFAOYSA-N 2-methyltetradecan-4-one Chemical compound CCCCCCCCCCC(=O)CC(C)C YVVVNAZSGGAAPW-UHFFFAOYSA-N 0.000 description 1
WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical compound CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 description 1
FLKHCKPUJWBHCW-UHFFFAOYSA-N 3,6-dichlorophthalic acid Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1C(O)=O FLKHCKPUJWBHCW-UHFFFAOYSA-N 0.000 description 1
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239000004215 Carbon black (E152) Substances 0.000 description 1
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FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
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244000147568 Laurus nobilis Species 0.000 description 1
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229910002651 NO3 Inorganic materials 0.000 description 1
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239000004743 Polypropylene Substances 0.000 description 1
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IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 1
KYIKRXIYLAGAKQ-UHFFFAOYSA-N abcn Chemical compound C1CCCCC1(C#N)N=NC1(C#N)CCCCC1 KYIKRXIYLAGAKQ-UHFFFAOYSA-N 0.000 description 1
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239000007767 bonding agent Substances 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
238000012662 bulk polymerization Methods 0.000 description 1
239000001273 butane Substances 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
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238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000003595 mist Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000003607 modifier Substances 0.000 description 1
OKRNLSUTBJUVKA-UHFFFAOYSA-N n,n,n',n'-Tetrakis(2-hydroxyethyl)adipamide Chemical compound OCCN(CCO)C(=O)CCCCC(=O)N(CCO)CCO OKRNLSUTBJUVKA-UHFFFAOYSA-N 0.000 description 1
ZWWQICJTBOCQLA-UHFFFAOYSA-N o-propan-2-yl (propan-2-yloxycarbothioyldisulfanyl)methanethioate Chemical compound CC(C)OC(=S)SSC(=S)OC(C)C ZWWQICJTBOCQLA-UHFFFAOYSA-N 0.000 description 1
KPWVFNOPNOTYNJ-UHFFFAOYSA-N octadecyl benzoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC=CC=C1 KPWVFNOPNOTYNJ-UHFFFAOYSA-N 0.000 description 1
150000002923 oximes Chemical class 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
229960000964 phenelzine Drugs 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
QCCDLTOVEPVEJK-UHFFFAOYSA-N phenylacetone Chemical compound CC(=O)CC1=CC=CC=C1 QCCDLTOVEPVEJK-UHFFFAOYSA-N 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
238000010526 radical polymerization reaction Methods 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
229940070710 valerate Drugs 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Chemical group 0.000 description 1
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09D133/062—Copolymers with monomers not covered by C09D133/06
- C09D133/064—Copolymers with monomers not covered by C09D133/06 containing anhydride, COOH or COOM groups, with M being metal or onium-cation
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Paints Or Removers (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Macromonomer-Based Addition Polymer (AREA)
Organic Insulating Materials (AREA)
Laminated Bodies (AREA)
Polyurethanes Or Polyureas (AREA)
Phenolic Resins Or Amino Resins (AREA)
Developing Agents For Electrophotography (AREA)
Surface Treatment Of Glass Fibres Or Filaments (AREA)

TW090101825A 2000-01-31 2001-01-30 Thermosetting coating materials TWI254068B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE10004136A DE10004136C2 (de)	2000-01-31	2000-01-31	Wärmehärtbare Beschichtungsmassen

Publications (1)

Publication Number	Publication Date
TWI254068B true TWI254068B (en)	2006-05-01

Family

ID=7629320

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW090101825A TWI254068B (en)	2000-01-31	2001-01-30	Thermosetting coating materials

Country Status (18)

Country	Link
US (1)	US6946088B2 (cs)
EP (1)	EP1261670B1 (cs)
CN (1)	CN1164704C (cs)
AT (1)	ATE249504T1 (cs)
AU (1)	AU782348B2 (cs)
CA (1)	CA2398098C (cs)
CZ (1)	CZ300613B6 (cs)
DE (2)	DE10004136C2 (cs)
DK (1)	DK1261670T3 (cs)
ES (1)	ES2206422T3 (cs)
MX (1)	MXPA02007353A (cs)
MY (1)	MY128640A (cs)
NO (1)	NO327261B1 (cs)
PL (1)	PL204394B1 (cs)
PT (1)	PT1261670E (cs)
RU (1)	RU2249605C2 (cs)
TW (1)	TWI254068B (cs)
WO (1)	WO2001057148A1 (cs)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1319698A1 (en) *	2001-12-12	2003-06-18	Dsm N.V.	Method for hotmelt application
JP4104931B2 (ja) *	2002-07-29	2008-06-18	ジョンソンディバーシー株式会社	水性床用樹脂分散体およびそれを用いたフロアーポリッシュ組成物
DE102006009511A1 (de) *	2006-02-28	2007-08-30	Röhm Gmbh	Synthese von Polyester-pfropf-Poly(meth)acrylat
EP1835000A1 (en) *	2006-03-17	2007-09-19	Cytec Surface Specialties Austria GmbH	Aqueous binders for coatings with improved gloss
CN102161626A (zh) *	2011-02-22	2011-08-24	合肥工业大学	一种含两个丙烯酸酯的二酰胺化合物及其制备方法和用途
CN105765004B (zh) *	2013-11-25	2019-04-09	宣伟投资管理有限公司	用于高填充粉末涂料的聚酯树脂
CA2986429C (en) *	2015-05-26	2020-03-10	Saint-Gobain Adfors Canada, Ltd.	Glass mat reinforcement

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Publication number	Priority date	Publication date	Assignee	Title
DE2418976C3 (de) *	1974-04-19	1978-10-26	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung von wasserunlöslichen Kunstharzen mit Anionenaustauscher-Eigenschaften
US4305868A (en) *	1978-08-04	1981-12-15	Uniroyal, Inc.	Phenolic esteramide antioxidants
US4801680A (en) *	1987-12-30	1989-01-31	Ppg Industries, Inc.	Hydroxyalkylamide powder coating curing system
US5266657A (en) *	1991-05-29	1993-11-30	Rohm And Haas Company	Monocarboxylic acid power coating curing systems
US5216090A (en) *	1992-07-27	1993-06-01	Rohm And Haas Company	Fatty acid hydroxyalkylamides as coreactable stabilizers and flow aids for powder coatings
BE1006097A3 (nl)	1992-07-29	1994-05-10	Dsm Nv	Poederverf op basis van een polymeer met vrije carbonzuurgroepen als bindmiddel en een beta-hydroxyalkylamidegroepen bevattende verbinding als crosslinker.
US5471602A (en) *	1992-07-31	1995-11-28	Hewlett-Packard Company	System and method of scoreboarding individual cache line segments
DE4430400A1 (de)	1994-08-26	1996-02-29	Inventa Ag	Wärmehärtbares Beschichtungssystem aus mehreren Bindemittelharzen
DE4430399C1 (de) *	1994-08-26	1996-02-22	Inventa Ag	Epoxidfreies, wärmehärtbares Beschichtungssystem
US5744531A (en) *	1996-06-24	1998-04-28	Ppg Industries, Inc.	Anionic electrocoating compositions containing hydroxyalkylamide curing agents
ATE193045T1 (de) *	1996-10-30	2000-06-15	Inventa Ag	Wärmehärtbare beschichtungsmassen
AU721485B2 (en)	1996-10-30	2000-07-06	Ems-Patent Ag	Heat curable coating compounds
NL1007186C2 (nl)	1997-10-01	1999-04-07	Dsm Nv	ß-hydroxyalkylamide groepen bevattend condensatiepolymeer.

2000
- 2000-01-31 DE DE10004136A patent/DE10004136C2/de not_active Expired - Lifetime
2001
- 2001-01-29 DK DK01948906T patent/DK1261670T3/da active
- 2001-01-29 RU RU2002120484/04A patent/RU2249605C2/ru active
- 2001-01-29 ES ES01948906T patent/ES2206422T3/es not_active Expired - Lifetime
- 2001-01-29 PL PL356906A patent/PL204394B1/pl unknown
- 2001-01-29 AU AU28516/01A patent/AU782348B2/en not_active Expired
- 2001-01-29 EP EP01948906A patent/EP1261670B1/de not_active Expired - Lifetime
- 2001-01-29 AT AT01948906T patent/ATE249504T1/de active
- 2001-01-29 MX MXPA02007353A patent/MXPA02007353A/es active IP Right Grant
- 2001-01-29 CN CNB018043577A patent/CN1164704C/zh not_active Expired - Lifetime
- 2001-01-29 PT PT01948906T patent/PT1261670E/pt unknown
- 2001-01-29 DE DE50100608T patent/DE50100608D1/de not_active Expired - Lifetime
- 2001-01-29 US US10/182,695 patent/US6946088B2/en not_active Expired - Lifetime
- 2001-01-29 CZ CZ20022573A patent/CZ300613B6/cs not_active IP Right Cessation
- 2001-01-29 CA CA002398098A patent/CA2398098C/en not_active Expired - Lifetime
- 2001-01-29 WO PCT/EP2001/000938 patent/WO2001057148A1/de not_active Ceased
- 2001-01-30 MY MYPI20010399A patent/MY128640A/en unknown
- 2001-01-30 TW TW090101825A patent/TWI254068B/zh not_active IP Right Cessation
2002
- 2002-07-30 NO NO20023629A patent/NO327261B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
PL204394B1 (pl)	2010-01-29
EP1261670B1 (de)	2003-09-10
CN1396946A (zh)	2003-02-12
EP1261670A1 (de)	2002-12-04
CN1164704C (zh)	2004-09-01
CZ20022573A3 (cs)	2003-01-15
HK1053487A1 (en)	2003-10-24
DE50100608D1 (de)	2003-10-16
CA2398098A1 (en)	2001-08-09
CZ300613B6 (cs)	2009-07-01
RU2002120484A (ru)	2004-01-10
PL356906A1 (en)	2004-07-12
ES2206422T3 (es)	2004-05-16
WO2001057148A1 (de)	2001-08-09
CA2398098C (en)	2009-07-21
NO327261B1 (no)	2009-05-25
ATE249504T1 (de)	2003-09-15
NO20023629L (no)	2002-09-30
NO20023629D0 (no)	2002-07-30
AU2851601A (en)	2001-08-14
DE10004136A1 (de)	2001-08-09
DK1261670T3 (da)	2004-01-26
DE10004136C2 (de)	2001-11-29
RU2249605C2 (ru)	2005-04-10
MY128640A (en)	2007-02-28
AU782348B2 (en)	2005-07-21
US6946088B2 (en)	2005-09-20
MXPA02007353A (es)	2003-01-28
US20030130440A1 (en)	2003-07-10
PT1261670E (pt)	2004-02-27

Legal Events

Date	Code	Title	Description
2021-03-11	MK4A	Expiration of patent term of an invention patent

Publication	Publication Date	Title
US5266657A (en)	1993-11-30	Monocarboxylic acid power coating curing systems
US6184311B1 (en)	2001-02-06	Powder coating composition of semi-crystalline polyester and curing agent
ES2238492T3 (es)	2005-09-01	Composicion termoendurecible en polvo para revestimientos.
JP4132147B2 (ja)	2008-08-13	艶消し塗料組成物
TW200403311A (en)	2004-03-01	Semi-gloss powder coating compositions
US5741602A (en)	1998-04-21	Heat-curable coating composition comprising plurality of binder resins
GB2244060A (en)	1991-11-20	Powder coating compositions containing semi-crystalline polyesters
US6180726B1 (en)	2001-01-30	High temperature resistant coating composition and method of using thereof
US5216090A (en)	1993-06-01	Fatty acid hydroxyalkylamides as coreactable stabilizers and flow aids for powder coatings
TWI254068B (en)	2006-05-01	Thermosetting coating materials
US5153252A (en)	1992-10-06	Thermosetting powder coating compostions containing bisphenoxy-propanol as a melt viscosity modifier
US7041737B2 (en)	2006-05-09	Coating powder composition, method of use thereof, and articles formed therefrom
TW568924B (en)	2004-01-01	Polyester containing tertiary carboxyl groups, process for its preparation and thermosetting powder compositions containing it
US5342893A (en)	1994-08-30	Antipopping agents for powder coating compositions
US20050288450A1 (en)	2005-12-29	Coating matting agent comprising amide condensation product
JPH07509504A (ja)	1995-10-19	熱硬化性粉体塗料組成物
JP2003183573A (ja)	2003-07-03	熱硬化型艶消し粉体塗料
JP2004292566A (ja)	2004-10-21	樹脂組成物